Lake Region Medical
ANCHORWIRE GUIDEWIRE
SKU K111288UPC DQX
In Stock
—
IIFDA 510(k) Cleared (K111288)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Lake Region Medical
Free shipping on orders over $99 · 30-day returns
ANCHORWIRE GUIDEWIRE is an FDA 510(k)-cleared medical device (K111288) manufactured by Lake Region Medical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 1, 2011. Regulation: 8.
